Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77910Generated: October 29, 2026

Nitromethane → 2-Methyl-5-(4-((E)-2-nitro-vinyl)-benzyl)-furan

https://huagongshe.com/reaction/77910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
ReactantAmmonium AcetateHCID 517165—
Reactant4-(5-Methyl-furan-2-ylmethyl)-benzaldehydeHCID 59255265—
SolventAcetic AcidHCID 176—
Product2-Methyl-5-(4-((E)-2-nitro-vinyl)-benzyl)-furanHCID 59255436102.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 4-(5-methyl-furan-2-ylmethyl)-benzaldehyde (96 mg, 0.48 mmol) described in Manufacturing Example 46-1-3 and acetic acid (1 mL) were added nitromethane (190 μL, 3.6 mmol) and ammonium acetate (110 mg, 1.4 mmol) at room temperature, which was stirred for 3 hours at 100° C. The reaction mixture was cooled to room temperature, and extracted by addition of water and ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and dried over magnesium sulfate. The filtrate was concentrated under a reduced pressure to obtain the title compound (120 mg) as a crude product. This compound was used in the following reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841327B2
Source datasetuspto-grants-2014_09
ORD IDord-23699884cf104bee98fc65c0ddaefd81
Source noteuspto-grants-2014_09